Write the mechanism for all combinations of reactions given in this handout (attached below). Include stereochemistry when possible. Write and E2 Alkyl halides: Br Bor Br Br Br BV Ban/NU: t-Buok, Nao Et NaH
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If possible to draw mechanisms and products for the second row of compounds
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- If possible to draw mechanisms of each combo for just the first row of compoundsDraw structural formulas for all of the enol forms of the carbonyl compound below3c)Referring to the intermediates you drew in problem below explain in detail why no meta product is obtained in the Friedel-Crafts alkylation of chlorobenzene. Draw all pertinent resonance structures to support your argument.
- If possible to draw the mechanisms and products of the last row of compounds for all nu:Give detailed mechanism Solution with explanation needed..don't give Handwritten answerGive detailed mechanism Solution with explanation needed..don't give Handwritten answer..give also type of reaction..SN1 ,SN2, E1 and E2
- d) In any Friedel-Crafts alkylation reaction starting with benzene and using one equivalent of the alkylating reagent, there is a always a small amount of disubstituted product which is formed. By contrast, such outcomes are not typically observed for any halogenation reactions starting from benzene and similarly using EAS chemistry. Please explain the basis for this apparent dichotomy.Draw structural formulas for all of the enol forms of the carbonyl compound below3. For the following variants of the rearrangement reactions we have covered in class, propose a feasible step-by-step mechanism for each of them. (a) NaOMe MeOH
- Give detailed Solution with explanation needed..please explain....for a good reviewGive detailed mechanism Solution with explanation needed of each steps....don't give Handwritten answer...reaction type SN1, SN2,E1 E2Give detailed mechanism Solution with explanation needed..don't give Handwritten answer